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. 2016 Feb 4;7(9):10182–10192. doi: 10.18632/oncotarget.7186

Table 2. Summary of chromosomal rearrangements by whole genome sequencing analysis in LM200-#25.

ID Break 1 Chromosome Break 1 Position Break 2 Chromosome Break 2 Position Rearrangement Type Sequence in Between Breakpoints
23 2 15,742,392 2 16,708,640 RF CTGAA insertion
29 2 48,937,454 2 81,807,507 RF C microhomology
30 2 53,106,380 2 53,252,037 LD AA microhomology
50 3 144,705,944 12 28,795,184 CT TT microhomology
76 5 6,330,710 5 6,378,473 RF TG microhomology
80 5 19,854,137 5 89,613,562 LD
91 5 89,613,939 20 14,453,942 CT TGGA microhomology
93 5 95,994,652 5 96,157,380 RF GAT microhomology
108 7 26,274,055 7 123,601,513 LD
109 7 51,228,098 7 51,281,802 RF TT microhomology
119 7 127,757,875 7 127,820,864 FF TTT microhomology
120 7 127,757,880 11 23,404,604 CT
143 12 53,845,481 20 5,707,700 CT G microhomology
167 20 57,562,329 20 57,708,236 LD GCTCTGGTCCTGCATGACGTCCGTAGGATCACTT insertion

*Bold numbers indicate that several breakpoints were located in close proximity

CT

chromosomal translocation

LD

long deletion

FF

forward and forward

RF

reverse and forward