[86C7-86C7];[86E11-86E11];
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;86E11;[86C7-86C7];[86E11-86E11];
86C7;86E11
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Inferred to overlap with: Df(3R)MS32.
Lethal in combination with Df(3R)MS32.
Flies heterozygous for the deletion show a Minute bristle phenotype.
Shows 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 of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP3340EP3340 and P{PZ}tho1&P{PZ}l(3)0462905275 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}tho1&P{PZ}l(3)0462905275 and P{EP}Lk6EP886