Correlation pattern between molecular mutations and karyotype. Data are given for associations between BCOR mutations and DNMT3A, NPM1, FLT3-ITD, CEBPA, MLL-PTD, RUNX1, and IDH1 and IDH2 mutations in 160 patients (top panel). The association between BCOR mutations and entity-defining cytogenetic abnormalities (40 patients) is shown in the bottom panel.