Fig. 1From: Double inv(3)(q21q26.2) in acute myeloid leukemia is resulted from an acquired copy neutral loss of heterozygosity of chromosome 3q and associated with disease progressionKaryotypes from patient a showing 46,XY,inv(3)(q21q26.2) at the diagnosis and b 46,XY,inv(3)(q21q26.2)x2 at disease progression. ACGH + SNP showed evidence of aCN-LOH of chromosome 3q c whole genome view and d chromosome 3 only with 3q highlighted in light blueBack to article page