[42F2-42F2];[43C1-43C1];
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.
42F2;43C1
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Lethal in combination with Df(2R)ED1673.
The presence of P+PBac{XP5.RB3}BSC263 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(2R)BSC263 predicted from the Release 4 genomic coordinates of the progenitor P{XP}d04819 and PBac{RB}CG30502e00486 transposable element insertions sites are 42F2;43C1.