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.
Inferred to overlap with: Df(3L)Exel6084.
The breakpoints of Df(3L)BSC835 predicted from the Release 5 genomic coordinates of the insertion sites of the progenitor transposable elements P{XP}d10863 and PBac{WH}f01995 are 3L:276882 ;381004 and the cytological breakpoints predicted from these coordinates are 61B3;61C1.