[26B2-26B2];[26D7-26D7];
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.
26B2;26D7
Inferred to overlap with: Df(2L)BSC239.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}chicEP713&P{EP}chicEP1095 and P{lacW}Gef26k13720 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k09923k09923&P{lacW}CG9523k07502b and P{EP}Sec61αEP2180