This option is used to check if a repeated sequence could
be involved in the mutational event. The repeated sequences is
usually localized at each extremity of the deletion. This situation
if found habitually when a deletion involving more than 2 nt
is present. When the deletion involves only 1 nt, it is mostly
localized in a stretch of this nucleotide (polyC for example).
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Choose UMD databases to use for this analysis: |