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.
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
The presence of P+PBac{XP5.WH5}BSC739 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(3R)BSC739 predicted from the Release 5 genomic coordinates of the insertion sites of the progenitor transposable elements P{XP}d09030 and PBac{WH}ALiXf03094 are 97E1;98B1.