[39F3-39F3];[40D3-40D3];
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.
39F3;40D3
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(2L)Exel6049.
Lethal in combination with: Df(2L)Exel6049.
Presence of P+PBac{XP5.WH5}BSC150 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(2L)BSC150 predicted from the transposable element insertions sites using Release 3 coordinates are 39F3;40D3.