[36F7-36F7];[37A1-37A1];
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.
36F7;37A1
Breakpoint based on release 3 sequence coordinate from Thibault et al., 2004, Supplementary Table 2 (FBrf0174227) or 3 (FBrf0174228), converted to release 5 coordinate.
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(2L)Exel7071.
Fails to complement Df(2L)Exel7071 and Df(2L)OD15.
Chromosome lacks miniwhite markers.
The cytological breakpoints of Df(2L)BSC112 predicted from the Release 3 genome coordinates of the progenitor insertions are 36F7;37A1.