[30F5-30F5];[31B1-31B1];
A set of ~50 targeted deficiencies created by exploiting hybrid element insertion (HEI) and resolution; designed to fill gaps in deletion coverage.
30F4-30F5;31B1-31B4
30F5;31B1
The 2L:10200998 release 6 coordinate of the left breakpoint is an estimate. It corresponds to the insertion site of P{EPgy2}EY03684. As FBrf0175003 explains, deletions generated by P transposase in the presence of trans-heterozygous P elements are expected to extend from the end of one P insertion to the vicinity of the other P insertion. Heterozygosity for Df(2L)BSC17 does not cause Minute phenotypes, so the right breakpoint must lie to the left of the haploinsufficient RpL7 gene.
The 2L:9984170 release 6 coordinate of the left breakpoint is an estimate. It corresponds to the insertion site of P{EP}CR13130EP2238. As FBrf0175003 explains, deletions generated by P transposase in the presence of trans-heterozygous P elements are expected to extend from the end of one P insertion to the vicinity of the other P insertion.
The deficiency chromosome retains the miniwhite marker from P{EP}CG13130EP2238 and/or P{EPgy2}EY03684.