[16C1-16C1];[16F6-16F6];
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.
16C1;16F6
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
The presence of P+PBac{XP5.WH5}BSC647 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(1)BSC647 predicted from the Release 5 genomic coordinates of the progenitor insertions are 16C1;16F6.
The presence of a deletion was confirmed cytologically, though the breakpoints were not analyzed in detail.