Table 1.
Summary of cytogenetically verified inversion events
|
Fosmid coordinates, build 34a
|
Breakpoints defined in literature
|
|||||
|---|---|---|---|---|---|---|
| Chr. | Bp. 1 | Bp. 2 | Chr. | Bp. 1 | Bp. 2 | Reference |
| chr1 | 87,288,446-87,328,446 | 145,375,657-145,415,657 | chr1 | unpublished | ||
| chr4 | 44,709,174-44,749,174 | 86,393,839-86,434,839 | chr4 | 44,730,692-44,751,795 | 86,275,393-86,461,364 | (Kehrer-Sawatzki et al. 2005a) |
| chr5 | 18,582,661-18,622,611 | 95,031,126-96,011,126 | chr5 | 18,443,766-18,614,471 | 95,891,549-96,072,074 | (Kehrer-Sawatzki et al. 2005c) |
| chr9 | 40,749,944-40,789,944 | 84,288,147-84,328,147 | chr9 | unmapped | 84,256,135-84,387,819 | (Kehrer-Sawatzki et al. 2005c) |
| chr12 | 20,845,308-20,885,308 | 66,631,594-66,671,594 | chr12 | 20,833,482-21,009,087 | 66,627,151-66,740,912 | (Kehrer-Sawatzki et al. 2005b) |
| chr15 | 20,702,019-20,742,019 | 26,722,088-26,762,088 | chr15 | unmapped | 28,025,787-28,486,050 | (Locke et al. 2003a) |
| chr17 | 8,123,673-8,163,673 | 48,068,346-48,108,346 | chr17 | 8,128,215-8,139,694 | 48,037,665-48,224,281 | (Kehrer-Sawatzki et al. 2002) |
| chr18 | 121,769-161,769 | 16,735,019-16,775,019 | chr18 | 102,251-103,561 | 16,762,886-16,898,525 | (Goidts et al. 2004) |
(Chr.) Chromosome, (Bp) breakpoint.
a
Fosmid coordinates are a range based on the genomic distances between two fosmid ends that determine the breakpoint