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.
The presence of P+PBac{XP5.WH5}BSC799 was verified using the PCR methods and primers described in FBrf0175003.
The breakpoints of Df(3L)BSC799 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}bab1f02681 and P{XP}d07664 insertion sites are 3L:1074839 ;1247708 and the cytological breakpoints predicted from these coordinates are 61E3;61F4.