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}BSC842 was verified using the PCR methods and primers described in FBrf0175003.
The breakpoints of Df(3R)BSC842 predicted from the Release 5 genomic coordinates of the insertion sites of the progenitor transposable elements P{XP}d04917 and PBac{WH}Rrp6f07001 are 3R:10557249 ;10711196 and the cytological breakpoints predicted from these coordinates are 88D2;88D6.