[42A13-42A13];[42E6-42E6];
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.
42A13;42E6
Pld3.1/Df(2R)ED1612 transheterozygous adult flies display Light-induced retinal degeneration.
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(2)k09848k09848&P{EP}EP407 and P{lacW}geminink14019&P{PZ}Adf101349 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}vimark16722 and P{lacW}cosk16101