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.
Lethal in combination with Df(2R)Exel7177.
Inferred to overlap with: Df(2R)BSC777.
Carries two copies of a mini-w marker.
The cytological breakpoints of Df(2R)BSC698 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}f00012 and P{XP}CG9812d10315 insertion sites are 59C1;59D11.