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. 2020 Nov 30;29(4):637–648. doi: 10.1038/s41431-020-00770-0

Fig. 3. Interpretation of variation identified by LRS but not SRS.

Fig. 3

From left to right showing three groups: the number of genes of which coding regions are affected by an SV, the number genes affected by a putatively damaging SNV identified only in LRS, the number of genes of which coding regions are covered less than 10% in SRS but that do have coverage in LRS. Individual bars indicate different types of disorders based on diagnostic gene panels as used by Genome Diagnostics Nijmegen (https://www.radboudumc.nl/en/patientenzorg/onderzoeken/exome-sequencing-diagnostics/information-for-referrers/exome-panels), genetic testing laboratory. Numbers in the legend indicate the total number of genes in each of the gene panels.