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.
Inferred to overlap with: Df(3R)Exel7327.
Carries two copies of a mini-w marker.
The cytological breakpoints of Df(3R)BSC728 predicted from the Release 5 genomic coordinates of the progenitor P{XP}CG4221d08178 and PBac{RB}Mhcle03696 insertion sites are 89A8;89B2.