[12A9-12A9];[12C6-12C6];
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.
12A9;12C6
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}NFATEP1390&P{EP}CG11164EP1396 and P{EP}gEP514 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG33174EP1101 and P{EP}EP1595EP1595