[57F6-57F6];[57F10-57F10];
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.
57F6;57F10
Inferred to overlap with: Df(2R)BSC786.
Df(2R)ED3923 flies exhibit the loss of the distal portion of the L5 longitudinal vein with full penetrance.
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}CG10082EP436&P{EP}EP712EP712 and P{EP}Tim10EP541&P{lacW}l(2)k09617k09617 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}Tim10EP541&P{lacW}l(2)k09617k09617 and P{PZ}l(2)0783707837