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)XG5
Inferred to overlap with: Df(3L)ED218.
The breakpoints of Df(3L)BSC833 predicted from the Release 5 genomic coordinates of the P{XP}d05666 and PBac{WH}CG7304f05948 transposable element insertion sites are 3L:15507245--15507523 ;15671057 and the cytological breakpoints predicted from these coordinates are 71D4;71F1.