[89E13-89E13];[90C1-90C1];
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.
89E13;90C1
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG5208EP562&P{EP}DadEP3196 and P{PZ}l(3)0788207882 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)0788207882 and P{EP}cpoEP3679