[61C1-61C1];[61E2-61E2];
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.
61C2;61E2;[61C2-61C2];[61E2-61E2];
61C1;61E2
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Confirmed by PCR (using the 3-step process described on 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}trh10512 and P{EP}EP3104EP3104 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)0596705967 and P{PZ}l(3)0264002640