[42A8-42A8];[42A11-42A11];
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.
42A8;42A11
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS3}UM-8021-3 and P{RS5}5-HA-1968.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(2)0985109851&P{lacW}Src42Ak10108 and P{lacW}l(2)k09848k09848&P{EP}EP407 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k09848k09848&P{EP}EP407 and P{lacW}geminink14019&P{PZ}Adf101349