[38F1-38F1];[39A6-39A6];
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.
38F1;39A6
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(2L)Exel7080.
The presence of P+PBac{XP5.WH5}BSC333 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(2L)BSC333 predicted from the Release 5 genomic coordinates of the P{XP}CG31674d00365 and PBac{WH}E2f2f01466 transposable element insertions sites are 38F1;39A6.