[47A10-47A10];[47C1-47C1];
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.
47A10;47C1
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php 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}Hr46k10308 and P{PZ}lola00349&P{EP}lolaEP952 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k00909k00909&P{EP}EP2619EP2619 and P{lacW}l(2)k15826k15826&P{EP}EP471