| 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 |
