Extended Data Fig. 2: Recurrent inversions and translocations.

a, Number of samples with inversions (y axis) according to the genomic coordinates of the full chromosome from 5’ to 3’ on each chromosome (x axis), for each chromosome (panels). b-c, Distance between all inversion (b) and translocation (c) (breakpoints across all 485 samples on each chromosome highlighting hotspot breakpoints (named kataegis, in red).