Heatmap from Scientific Research

Oncoprint of genetic alterations enriched in each subtype. Samples are in the same order as in Fig. 1a. Molecular subtype, sample type (diagnosis/relapse) and gene mutations are shown for each sample. Alteration frequencies in each subtype are shown on the right. IKZF1 deletions include monosomy 7. Copy number gains from trisomy 21 are not included in RUNX1 alteration frequencies. In hyperdiploid cases, trisomy 21 is a consequence of the hyperdiploid state. Fisher’s exact test was performed using only diagnostic samples or all samples.

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