[17D1-17D1];[18C1-18C1];
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.
17D1;18C1
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP443EP443&P{EP}BxEP1383 and P{EP}Pk17EEP438 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG8051EP1550&P{EP}EP1300 and P{EP}EP1526&P{EP}PfrxEP1150