[42D6-42D6];[42F1-42F1];
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.
42D6;42F1
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
The presence of P+PBac{XP5.WH5}BSC262 was verified using the PCR methods and primers described in Parks et al.FBrf0175003.
The cytological breakpoints of Df(2R)BSC262 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}CG30158f06824 and P{XP}esnd07374 transposable element insertions are 42D6;42F1. The presence of a deletion was confirmed cytologically, though the breakpoints were not analyzed in detail.