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.
Lethal in combination with Df(2R)X58-12.
Inferred to overlap with: Df(2R)Exel6079.
The breakpoints of Df(2R)BSC787 predicted from the Release 5 genomic coordinates of the progenitor PBac{RB}e02534b and P{XP}d03340 transposable element insertion sites are 2R:18549332 ;18685826 and the cytological breakpoints predicted from these coordinates are 58F4;59B1.