A set of ~50 targeted deficiencies created by exploiting hybrid element insertion (HEI) and resolution; designed to fill gaps in deletion coverage.
22D1-22D3;22F1-22F2
The 2L:2175620 release 6 coordinate of the left breakpoint is an estimate. It corresponds to the insertion site of P{PZ}aop03953a. 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 2L:2450829 release 6 coordinate of the left breakpoint is an estimate. It corresponds to the insertion site of P{EP}dppEP2232. 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. It is unlikely sequences to the right of P{EP}dppEP2232 are deleted, because dpp is haplolethal.
Df(2L)OK371Δ fails to complement Df(2L)BSC37.
Inferred to overlap with: Df(2L)OK371Delta.
The deficiency chromosome retains the miniwhite marker from P{EP}dppEP2232.
Distal break between 22D1 and the 22D3,4 doublet; proximal break within the 22F1,2 doublet.