[29E1-29E1];[29F5-29F5];
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.
29E1;29F5
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{PZ}lmg03424 and P{lacW}Sema-1ak13702 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k04003k04003 and P{PZ}tai01351