Property | Value |
---|---|
% Polyploidy | 3.8 |
Ploidy Classification | hyperdiploid |
Modal Chromosome Number | 48.0 |
Modal Range Numeric | 43-49 |
Marker Chromosomes Average Field | None |
Primary or Metastasis | Primary |
Count of SV's | 13 |
ecDNA Present (Y/N/P): N
HSR Classification: N
ATCC Karyotype: No data
DSMZ Karyotype: human hyperdiploid karyotype with 3.8% polyploidy - 48(43-49)<2n>XY, +6, +8, der(1)inv(1)(p36q31)t(1;6) (q13;p12), der(2)t(2;17)(p23;q24.1)del(2)(q14.2q36), der(3)t(1;3)(p36;p25), ins(3;2)(q21;q14.2q36), t(5;8)(q11.2;q24), der(6)t(1;6)(q31;p12)t(3;6) (q26;q24), inv(12)(p13.3q13.2), t(13;14)(q32/33;q24.2), der(17)t(2;17)(p23;q24.1) - sideline with +der(5) - carries apparent variant translocations involving several ANLL breakpoints: 1p36, 3q21, 3q26 (megakaryocytic abnormalities), 12p13, 17q24 (FAB-M4)
Heterogeneity Indications and Other Notes: gene amplification suggested by large HSR - ch 17 nullisomy
ecDNA Amplicon Predicted: N
Predicted Amplicon Classes: ['Linear amplification']
View Feature 1 - OCIAML2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE Linear amplification
Class | Amplicon | Complexity Score |
---|---|---|
Linear amplification | 1 | 0.0 |
ecDNA: negative
No data