[14A8-14A8];[14B7-14B7];
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.
14A8;14B7
No eye phenotypes are seen in Df(1)BSC759/Df(1)ED7355 transheterozygotes.
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}Gβ13FEP1071 and P{EP}EP1458&P{EP}EP1522 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}kat80EP620&P{EP}cazEP1564 and P{EP}Cyp1EP1073&P{EP}Dsp1EP355