This tool can be used to view typical depth of sequence coverage obtained by exome sequencing performed by our laboratory. These data were calculated based on approximately 30 samples processed using our exome pipeline. An individual base is considered to have high coverage if the coverage was 20X or greater for at least half of the samples analyzed. Depth of coverage of a region of interest in a specific sample is not guaranteed. Please note, high coverage does not necessarily mean high quality data, as the sequence in some regions are not unique (more information about pseudogenes below).