Table 1 Supporting reads for 20 randomly selected translocations from the tumor in Fig. 6.

Translocation #	Position 1	Position 2	Supporting reads (approximate)	Total reads (exact)	% Support
1	3_65552053	2_20941004	10	61	16.39
2	2_161669843	18_78292047	10	119	8.40
3	15_43944218	1_112318855	6	89	6.74
4	13_23307876	11_88303305	11	104	10.58
5	5_5609182	18_56166475	14	77	18.18
6	5_7058436	2_8931319	4	49	8.16
7	16_83532604	14_96841358	15	83	18.07
8	3_153288050	17_10818207	15	88	17.05
9	16_83532819	14_96841377	19	94	20.21
10	16_18368004	12_80665928	10	85	11.76
11	8_102861241	17_67932443	0	57	0.00
12	14_21312516	11_9863013	16	234	6.84
13	9_55224433	8_85188141	13	82	15.85
14	X_38480149	9_55983052	12	70	17.14
15	6_73162349	16_96121815	3	34	8.82
16	4_43262573	3_113857214	4	68	5.88
17	5_62573934	13_86796353	2	77	2.60
18	3_135929183	1_139635092	9	95	9.47
19	6_67680744	4_147419479	0	158	0.00
20	7_79199005	19_40536086	14	81	17.28

Random translocations were selected by inputting all translocations from the tumor into Excel, and using the RAND() function to assign a random number.
The 20 highest translocations were then selected.
Positions 1 and 2 represent the translocation breakpoint.
Genome Ribbon was used to analyze read evidence.

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