[7C2-7C2];[7D1-7D1];
A set of ~800 largely isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Designed to fill gaps in deletion coverage and breakpoint placement; also used to replace older available deficiencies that have not been molecularly mapped.
7C2;7D1
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
1: P{XP}d08569
2: PBac{WH}CG15332f05798
The presence of P+PBac{XP5.WH5}BSC622 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(1)BSC622 predicted from the Release 5 genomic coordinates of the insertion sites of the progenitors P{XP}d08569 and PBac{WH}CG15332f05798 are 7C2;7D1.