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. Author manuscript; available in PMC: 2015 Apr 16.
Published in final edited form as: Cancer Res. 2014 Jun 1;74(11):3157–3167. doi: 10.1158/0008-5472.CAN-13-1727

Figure 2.

Figure 2

Mapping of breakpoints to the human genome. A, all breakpoints (dark green vertical lines) for the 28 samples mapping to each chromosome. Chromosomes are presented p to q arms (left to right) with the centromeres marked in red. Horizontal light green bars below each chromosome mark predicted chromosomal fragile sites described in ref. 16. B, breakpoints hitting chromosomes 1 and 8 for Lu12 lepidic. C–E, cases with breakpoints in common regions of chromosomes 12, 20, and 7 (respectively). INV, invasive; L, lepidic.