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(3R)BSC748.
The breakpoints of Df(3R)BSC792 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}f05986 and P{XP}Dadd02235 insertion sites are 3R:12808916..12808917 ;12890724 and the cytological breakpoints predicted from these coordinates are 89E5;89E11.