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(2L)ED784.
Inferred to overlap with: Df(2L)BSC340.
The cytological breakpoints of Df(2L)BSC768 predicted from the Release 5 genomic coordinates of the progenitor P{XP}Pectd06253 and PBac{WH}CG9305f04590 transposable element insertion sites are 34A9;34B8.