[28F5-28F5];[29B1-29B1];
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.
28F5;29B1
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)BSC228.
Inferred to overlap with: Df(2L)BSC235.
Inferred to overlap with: Df(2L)BSC200.
Lethal in combination with Df(2L)BSC200.
Inferred to overlap with: Df(2L)TE29Aa-11.
Fails to complement Df(2L)TE29Aa-11.
The cytological breakpoints of Df(2L)BSC111 predicted from the Release 3 genome coordinates of the progenitor insertions are 28F5;29B1.