[61C7-61C7];[62A2-62A2];
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.
61C7;62A2
Flies heterozygous for Df(3L)ED4196 display abnormal cardiac chamber sizes.
Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP3104EP3104 and P{PZ}l(3)0596705967 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}rhoEP3704&P{PZ}l(3)0622606226 and P{PZ}dlt04276