Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

Table 1 Coverage and sequencing statistics of 7 probands

Family ID	Proband no.	Initial bases on target	Base covered on target	Coverage of target region (%)	Mean depth on (×)	Fraction of target covered ≥4× (%)	Fraction of target covered ≥10× (%)	Fraction of target covered ≥20× (%)
JSNY-021	III3	335538	329163	98.10	190	96.69	94.10	92.60
JSNY-027	III4	335538	329834	98.30	188	97.00	95.80	93.50
JSNY-033	II3	335538	332518	99.10	264	97.56	95.30	93.60
JSNY-043	III3	335538	333189	99.30	259	98.00	96.10	94.80
JSNY-045	II3	335538	330675	98.55	223	97.39	95.70	93.30
JSNY-053	III4	335538	331089	98.67	199	98.19	96.20	94.50
JSNY-056	III1	335538	329965	98.34	245	96.96	94.50	92.30

ISSN: 1479-5876