[92A11-92A11];[92E2-92E2];
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.
92A11;92E2
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-HA-2055 and P{RS3}CB-6305-3.
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{EP}EP650 and P{PZ}l(3)1058510585 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)1058510585 and P{EP}SyndEP409