Case Report: Identification of an HNF1B p.Arg527Gln mutation in a Maltese patient with atypical early onset diabetes and diabetic nephropathy

Table 1 Whole exome sequencing detail of coverage and number of read

Number of reads in raw sequence	55,723,934
Number of reads after de-duplication	96.63%
Number of mapped reads	99.53%
Number of mapped reads to targeted regions of the genome	79.11%
Average depth	66.72%
Coverage 10×	98.67%
Coverage 20×	93.93%
Coverage 50×	58.10%

ISSN: 1472-6823