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Figure 6 | Molecular Cytogenetics

Figure 6

From: A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization

Figure 6

This is the screenshot from the UCSC genome browser for the fragment of 21q22.12 → 22.3. For Decipher Database, the entries of clinical cases are in red for deletions (mean log ratio < 0) and in blue for duplications (mean log ratio > 0). For Database of Genome Variants (DGV struct Var), inversions are in purple, whereas InDels are in blue if there is a gain in size relative to the reference, in red if there is a loss in size or in brown if there are reports of both a loss and a gain in size.

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