| Homo sapiens |
SRX14474687 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX8132768 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX14474693 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474692 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474691 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: Normal chromosomes N3, N4, N9, N13, N14, and X may be absent. The markers der(11)t(11;?)(q25;?) (M1); der(1)t(1;3)(p22?;p13?) (M2); and der(2)t(2;?) (q37;?) (M5) were detected by W.A. Nelson-Rees, et al., Int. J. Cancer 16: 74-85, 1975. |
NEB |
TNBC;Carcinoma |
NA |
| Homo sapiens |
SRX8960126 |
SRP277895 |
9606 |
HeLa |
cell line: HeLa |
other |
NA |
NA |
| Homo sapiens |
SRX14474690 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: Normal chromosomes N3, N4, N9, N13, N14, and X may be absent. The markers der(11)t(11;?)(q25;?) (M1); der(1)t(1;3)(p22?;p13?) (M2); and der(2)t(2;?) (q37;?) (M5) were detected by W.A. Nelson-Rees, et al., Int. J. Cancer 16: 74-85, 1975. |
NEB |
TNBC;Carcinoma |
NA |
| Homo sapiens |
SRX8960125 |
SRP277895 |
9606 |
HeLa |
cell line: HeLa |
other |
NA |
NA |
| Homo sapiens |
SRX14474697 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474696 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474695 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474694 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid human, presumably female (X, abnormal X) with most chromosome counts in the hypotriploid range.; Normal chromosomes X, N2, N3, N7, N8, N10, and N22 are clearly under-represented due to their involvement in the formation of the many marker (19) chromosomes present in this cell line.; A normal chromosome N1 (or two) is identified in each karyotype, but, in addition, regions of chromosome N1 are also present in five different marker chromosomes.; Variation is evident in the normal and marker chromosome copy number from karyotype to karyotype. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX8132770 |
SRP256946 |
9606 |
Ovaries |
tissue: Ovaries |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132774 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132773 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132772 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina |
NA |
NA |
| Homo sapiens |
SRX8132771 |
SRP256946 |
9606 |
Ovaries |
tissue: Ovaries |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132778 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132777 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132776 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX8132775 |
SRP256946 |
9606 |
Lung |
tissue: Lung |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX14474679 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid female (modal number = 64, range = 52 to 68), with chromosome counts in the near-triploid range. Normal chromosomes N8 and N15 were absent. Eleven stable rearranged marker chromosomes are noted as well as unassignable chromosomes in addition to the majority of autosomes that are trisomic. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474678 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid female (modal number = 64, range = 52 to 68), with chromosome counts in the near-triploid range. Normal chromosomes N8 and N15 were absent. Eleven stable rearranged marker chromosomes are noted as well as unassignable chromosomes in addition to the majority of autosomes that are trisomic. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474677 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid female (modal number = 64, range = 52 to 68), with chromosome counts in the near-triploid range. Normal chromosomes N8 and N15 were absent. Eleven stable rearranged marker chromosomes are noted as well as unassignable chromosomes in addition to the majority of autosomes that are trisomic. |
NEB |
TNBC;Adenocarcinoma |
NA |
| Homo sapiens |
SRX14474676 |
SRP364334 |
9606 |
Breast; Mammary gland |
karyotype: The cell line is aneuploid female (modal number = 64, range = 52 to 68), with chromosome counts in the near-triploid range. Normal chromosomes N8 and N15 were absent. Eleven stable rearranged marker chromosomes are noted as well as unassignable chromosomes in addition to the majority of autosomes that are trisomic. |
NEB |
TNBC;Adenocarcinoma |
NA |
