[12C4-12C4];[12E8-12E8];
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.
12C4;12E8
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Confirmed by 3-step PCR confirmation as shown in 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}CG33174EP1101 and P{EP}EP1595EP1595 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}l(1)G0007EP764 and P{EP}EP1599