[42E1-42E1];[43D3-43D3];
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.
42E1;43D3
Lethal in combination with Df(2R)BSC263.
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}vimark16722 and P{lacW}cosk16101 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG1600EP398 and P{PZ}scra03427&P{EP}EP2179