[47C5-47C5];[47D4-47D4];
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.
47C5;47D4
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Lethal in combination with Df(2R)BSC327.
Inferred to overlap with: Df(2R)ED2155.
Inferred to overlap with: Df(2R)Exel6059.
The presence of P+PBac{XP5.RB3}BSC314 was verified using the PCR methods and primers described in FBrf0175003 with the substitution of the primer 5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer in the Hybrid PCR protocol in the Supplementary Methods.
The cytological breakpoints of Df(2R)BSC314 predicted from the Release 5 genomic coordinates of the P{XP}CG30015d06273 and PBac{RB}e01872 transposable element insertions sites are 47C5;47D4.