Total SVs | 200 |
---|---|
Reference genome | Human chromosome 22 (Build 37 ref) |
Distribution of SV length | N(50, 5), N(80, 8), N(100, 10), N(120, 12), N(150, 15), N(170, 17), N(200, 20), N(400, 40) N(600, 60), N(800, 80), N (1000, 100) N(2000, 200), N(4000, 400) |
The rate of single nucleotide alterations | 1/10000 |
The number of tandem repeat | N(40, 20) (>1) |
Mean depth of coverage | 5, 10, 15, 20, 40 |
Read lengths | 50, 75, 100, 108 |
Distribution of template lengths | N(400, 50) |