| Homo sapiens |
ERX8012550 |
ERP135083 |
9606 |
NA |
INSDC status: public |
adapter_trimmed |
NA |
NA |
| Homo sapiens |
SRX2154274 |
SRP078144 |
9606 |
OVARY |
karyotype: This is a hypodiploid human cell line. The modal chromosome number was 43, occurring in 63.3% of cells. The range was 42 to 45. The rate of higher ploidies was 32%. The del(1)(q21), der(13)t(1;?;13) (q11;?;q34), der(11)t(11;?) (q12), del(10)(q22) and 3 other marker chromosomes were common to most cells, and 3 others were found only in some cells. One N11 had the HSR segment from p11 to the distal end. The normal N10, N12, N15, N17 and N19 were absent. Others were either single or paired. There were from 1 to 6 rearranged and unassignable chromosomes. The X chromosome was either single or paired |
Illumina |
ADENOCARCINOMA |
NA |
| Homo sapiens |
ERX8012551 |
ERP135083 |
9606 |
NA |
INSDC status: public |
adapter_trimmed |
NA |
NA |
| Homo sapiens |
SRX2154275 |
SRP078144 |
9606 |
PANCREAS |
karyotype: (P7) hypotriploid with abnormalities including dicentrics, breaks, acrocentric fragments, large submetacentric and subtelocentric chromosomes plus minute marker |
Illumina |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX2154278 |
SRP078144 |
9606 |
COLON |
karyotype: The stemline chromosome number is near diploid with the modal number at 45 (62%) and polyploids occurring at 6.8%. The markers 10q+ and t(?8p;18q) are present in all metaphases and t(9q;?16p-), in 80% of the cells karyotyped. N16 is monosomic in the presence of, but disomic in the absence of t(9q;?16p-). N10 and N18 are monosomic and other chromosomes from those mentioned above are disomic. Q-band observations revealed the presence of the Y chromosome, but not in all cells (50% of cells lacked the Y in G-band karyotypes) |
Illumina |
CARCINOMA |
NA |
| Rattus norvegicus |
SRX9075446 |
SRP280104 |
10116 |
Kidney |
treatment: Casein |
Illumina |
NA |
NA |
| Homo sapiens |
SRX2154279 |
SRP078144 |
9606 |
LUNG |
karyotype: Modal number = 79; range = 71 to 83 This is a hypertriploid human cell line with the modal chromosome number of 79, occurring in 20% of cells. The rate of cells with a higher ploidy was 5.5%. Karyotypes were very complex. There were over 22 marker chromosomes commonly present in most cells, many with complex structural rearrangements. Among these markers were: double copies for t(10qter--10q11.2::?::13C--13qter) and der(9)t(3;9) (p12;p22?), and one copy each for del (1) (p22) and i (iq). There were two normal X chromosomes per cell. Normal chromosomes Y, N1, N5, N14, and N15 were not found. Chromosomes N20 and N22 generally had four or more copies per cell |
Illumina |
ADENOCARCINOMA |
NA |
| Rattus norvegicus |
SRX9075447 |
SRP280104 |
10116 |
Adipose |
treatment: Casein |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX9075444 |
SRP280104 |
10116 |
Brain |
treatment: Casein |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX9075445 |
SRP280104 |
10116 |
Liver |
treatment: Casein |
Illumina |
NA |
NA |
| Homo sapiens |
SRX4029529 |
SRP144441 |
9606 |
Serum |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX2154272 |
SRP078144 |
9606 |
SKIN |
karyotype: (P6) hypodiploid to hypertetraploid with abnormalities including dicentrics, secondary constrictions and large telocentric marker. Note: Cytogenetic information is based on initial seed stock at ATCC. Cytogenetic instability has been reported in the literature for some cell lines |
Illumina |
MALIGNANT MELANOMA |
NA |
| Homo sapiens |
SRX2154273 |
SRP078144 |
9606 |
OVARY |
tissue: OVARY |
Illumina |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX2154270 |
SRP078144 |
9606 |
COLON |
karyotype: modal number = 71; range = 68 to 72. The stemline chromosome number is hypertriploid with the 2S component occurring at 2.4%. Seventeen marker chromosomes are found in most metaphases, generally in single copy per chromosome. The marker designations are: M1p-(=t(3p-;?) with a deleted short arm), t(7q;?), t(10q;?), i(13q), 19q+a; M6, ?t(8q;9q-), ?Xp, M9, 6q+, t(13;?)a, t(13;?)b, 19q+b, M14, M15, 15p+, and Xq-. Chromosome 13 is nullisomic and chromosomes 8 and 14 are generally monosomic. No Y chromosome was detected by QM band analysis |
Illumina |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX2154271 |
SRP078144 |
9606 |
SKIN |
tissue: SKIN |
Illumina |
MALIGNANT MELANOMA |
NA |
| Homo sapiens |
SRX4029534 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029535 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029532 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029533 |
SRP144441 |
9606 |
Serum |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029538 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029539 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029536 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
SRX4029537 |
SRP144441 |
9606 |
Plasma |
condition: Healthy Subject |
Illumina_2 |
NA |
NA |
| Homo sapiens |
ERX8012558 |
ERP135083 |
9606 |
NA |
INSDC status: public |
adapter_trimmed |
NA |
NA |
| Homo sapiens |
ERX8012559 |
ERP135083 |
9606 |
NA |
INSDC status: public |
adapter_trimmed |
NA |
NA |
