Fig. 4

a Characterization of KAIMRC1 cells by flow cytometry. A panel of biomarkers were used to characterize the cells. b Representative Karyogram of KAIMRC1 cells. Patient karyotyping revealed presence of a composite complex karyotype including; trisomy of chromosomes X,2,3,5,6,7,8,9,10,11,12,14,15,16,17,18,19,20,21 and 22; tetrasomy of chromosomes X,2,5,6,12,17,20,21,and 22; pentasomy of chromosomes 21, and 22; additional chromosomal material on chromosomes X(p22.3),1(q44)(×2), 8(p21),11(p15); deletion of chromosome 3(q21); and additional two marker chromosomes cannot be identified. These numerical and structural chromosomal abnormalities with multi-clonality suggests existence of heterogeneity of genomic instability in this patient