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.
Carries two copies of a mini-w marker.
The cytological breakpoints of Df(2R)BSC699 predicted from the Release 5 genomic coordinates of the progenitor P{XP}d01597 and PBac{RB}e01191 insertion sites are 48D7;48E6.