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.
An incorrect sequence location for breakpoint 2 of X:16 ,629,054 (Release 5), and incorrect estimated cytology for breakpoint 2 of 15A3, was displayed on FlyBase through to the FB2009_10 release.
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Heterozygotes do not display a Minute phenotype.