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)ED6076.
The presence of P+PBac{XP5.WH5}BSC805 was verified using the PCR methods and primers described in FBrf0175003.
The breakpoints of Df(3R)BSC805 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}Gr93af01688 and P{XP}PyKd05959 insertion sites are 3R:17659537 ;18193695..18193698 and the cytological breakpoints predicted from these coordinates are 93F13;94A6.