[75F2-75F2];[76A1-76A1];
A set of 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. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
75F2;76A1
Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(3)j4E6j4E6 and P{EP}MESR6EP3142 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}MESR6EP3142 and P{lacW}l(3)L3809L3809