[18A3-18A3];[18C2-18C2];
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.
18A3;18C2
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}CG7326EP1133 and P{EP}CG7502EP1326 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