[69C4-69C4];[69E8-69E8];
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.
69C4;69E8
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
The presence of P+PBac{XP5.WH5}BSC381 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(3L)BSC381 predicted from the Release 5 genomic coordinates of the PBac{WH}CG10638f01666 and P{XP}CG14118d06432 transposable element insertions sites are 69C4;69E8.