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SV/CNV Prediction

The structural variations (SV) and copy number variations (CNV) module may be employed in combination with a resequencing study to discover genome rearrangements in comparison to the reference.
Table 1: This detail of a results table lists putative structural variations.

Figure 1: This figure depicts a possible copy number variation in relation to a reference sample.

Standard modules where the SV/CNV module can be used: