| Property | Value |
|---|---|
| % Polyploidy | None |
| Ploidy Classification | hyperdiploid |
| Modal Chromosome Number | 49.0 |
| Modal Range Numeric | 46-51 |
| Marker Chromosomes Average Field | 3.0 |
| Primary or Metastasis | Primary |
| Count of SV's | 8 |
ecDNA Present (Y/N/P): N
HSR Classification: N
ATCC Karyotype: modal number = 49; range = 44 to 51. This is a hyperdiploid human cell line with the modal chromosome number of 49 occurring in 34% of cells. However, cells with 50 chromosomes also occurred at high percentage (24%). At least 11 markers were consistently present in most cells. Among them were: der(3)t(3;12) (q21;q13); del(3) (q21); inv(1) (p36.1q21), and der(16)t(5;16) (q13;p13.3), all present in single copy per cell. At least three Y-autosome markers were detected. Single normal X chromosome was found in every cell. Normal Y chromosome was not found.
DSMZ Karyotype: human flat-moded hyperdiploid karyotype - 49(46-51)<2n>XY, +7, +2-4mar, add(Y)(q12), add(3)(q2?7), del(3)q13), add(8)(p11), ?idic(9)(q3?4.2)del(9) (q1?q2?)add(9)(p11), t(11;22)(q24;q12), add(12)(p13), del(16)(q21) - carries t(11;22) effecting EWS-FLI1 fusion yielding longer type II RT-PCR transcript
Heterogeneity Indications and Other Notes: carries t(11;22) effecting EWS-FLI1 fusion yielding longer type II RT-PCR transcript
ecDNA Amplicon Predicted: N
Predicted Amplicon Classes: []
No features detected.
ecDNA: None
No data