[47B7-47B7];[47F1-47F1];
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.
47B7;47F1
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
The presence of P+PBac{XP5.WH5}BSC639 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(2R)BSC639 predicted from the Release 5 genomic coordinates of the insertions sites of the progenitor transposable elements PBac{WH}stanf00907 and P{XP}d01591 are 47B7;47F1.