TABLE 8.
FDD deletions
| Chromosome | Coverage (bp) | Chromosome length (bp) | % coverage | Deficiency: eye color | Deficiency: no color |
|---|---|---|---|---|---|
| 2L | 22,339,638 | 22,407,834 | 99.70 | 12,635 | 82,537 |
| 2R | 20,352,238 | 20,766,785 | 98.00 | 15,389 | 97,121 |
| 3L | 23,263,549 | 23,771,897 | 97.86 | 14,077 | 88,543 |
| 3R | 27,888,207 | 27,905,053 | 99.94 | 15,852 | 100,147 |
| 4 | 1,217,178 | 1,281,640 | 94.97 | 209 | 2,374 |
| X | 22,072,705 | 22,224,390 | 99.32 | 15,422 | 89,903 |
| Total | 117,133,515 | 118,357,599 | 98.97 | 73,584 | 460,625 |
This table is a summary of the FRT-derived deletions possible when the DrosDel and Exelixis collections of FRT-bearing inserts are combined. The total possible coverage for each chromosome arm is indicated as are the number of deletions that can be identified phenotypically (“eye color”) and those that require molecular identification (“no color”).