[102A1-102A1];[102A6-102A6];
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.
102A1;102A6
Df(4)ED6366 does not uncover hybrid sterility when heterozygous in males containing the D.simulans 4th chromosome introgressed into an otherwise D.melanogaster background.
Does not show a Minute phenotype.
Chromosome shows a dominant Minute phenotype.
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{SUPor-P}KG01127/PBac{5HPw+}A173 and PBac{5HPw+}A437 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{SUPor-P}CrkKG00336/P{SUPor-P}KG00711 and P{SUPor-P}KG02769