[86C7-86C7];[86D5-86D5];
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.
86C7;86D5;[86C7-86C7];[86D5-86D5];
86C7;86D5
Inferred to overlap with: Df(3R)MS32.
Lethal in combination with Df(3R)MS32.
Does not show a Minute phenotype: analysis aimed at identification of M(3)86D.
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.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP3340EP3340 and P{PZ}tho1&P{PZ}l(3)0462905275