[13E1-13E1];[13F17-13F17];
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.
13E1;13F17
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
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}CG6340EP1109&P{EP}l(1)G0168EP491 and P{EP}EP1489 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}Gβ13FEP1071 and P{EP}EP1458&P{EP}EP1522