[17B1-17B1];[18B2-18B2];
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.
17B1;18B2
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
The presence of P+PBac{XP5.WH5}BSC585 was verified using the PCR methods and primers described in FBrf0175002
The cytological breakpoints of Df(1)BSC585 predicted from the Release 5 genomic coordinates of the PBac{WH}f04282 and P{XP}d02762 transposable element insertions sites are 17B1;18B2.