Summary data for familial pancreatic cancer families with inactivating ATM variants
| Type | Family | Individual | Read length | Bases mapped to genome | Bases mapped to exome | Exome bases with ≥ 10 reads | Average raw coverage | Effective coverage | Total number of variants | Variants in SNP database |
|---|---|---|---|---|---|---|---|---|---|---|
| Whole-genome sequencing | FPC-A | 1 | 100 | 115,388,854,300 | 1,294,030,427 | 34,681,602 | 35 | 95.1% | 6,024,866 | 3,758,900 |
| 2 | 100 | 110,742,763,000 | 1,219,892,546 | 34,328,889 | 33 | 94,7% | 6,181,369 | 3,793,150 | ||
| 3 | 100 | 112,771,643,500 | 1,271,909,140 | 34,656,841 | 34 | 95.1% | 6,190,892 | 3,783,971 | ||
| Whole-exome sequencing | FPC-B | 1 | 75 | 8,110,266,675 | 4,118,378,295 | 36,458,593 | 109 | 97.9% | 35,674 | 19,573 |
| 2 | 75 | 7,597,985,850 | 4,076,171,309 | 36,560,365 | 108 | 98.0% | 35,724 | 19,605 | ||
| 3 | 75 | 5,649,542,100 | 2,815,928,672 | 36,067,752 | 74 | 97.6% | 34,923 | 19,554 |