[63C1-63C1];[63F5-63F5];
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.
63C1;63F5
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{PZ}l(3)0680306803 and P{PZ}kst01318 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}kst01318 and P{PZ}Sc205634