Files in this Data Supplement:

• Supplemental file 1 - Tables S1 (Rearrangements recovered in the GCR assay), S2 (Homologous recombination defects influence frequency rearrangements into essential genes), S3a (Rearrangement products observed more than once), S3b (Rearrangements involving the same last identifiable chromosome V position), S3c (Rearrangements involving the same genomic target position), and S4 (Recurrent rearrangements with potential selective advantage); Fig. S1 (Distribution of rearrangements on chromosome V), S2 (Rearrangements with longer junction identity lengths), S3 (BCR/ABL and EWS/FLI fusion breakpoints), S4 (Identities of isochromosomes observed in certain cancer types), S5 (Replication timing and target site selection), and S6 (Replication origin and termination zone position effects on target site selection; and supplemental references
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