[12F4-12F4];[13A5-13A5];
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.
12F4;13A5
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php
Limits computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP334&P{EP}EP977 and P{EP}hiwEP1305