16p13.11 copy number variation syndrome (Homo sapiens)

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<?xml version="1.0" encoding="UTF-8"?> <Pathway xmlns="http://pathvisio.org/GPML/2013a" Name="16p13.11 copy number variation syndrome " Version="20241108" Organism="Homo sapiens"> <Comment Source="WikiPathways-description">Copy number variations in the region 16p13.11 (exact position: chr16:15511655-16293689 (GRCh37), are rare, pathological mutations in the human genome. 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Database="Ensembl" ID="ENSG00000204843" /> </DataNode> <DataNode TextLabel="PCM1" GraphId="faa2b" Type="GeneProduct"> <Comment>Pericentriolar Material 1 Protein</Comment> <Graphics CenterX="575.497481794958" CenterY="945.5625652935433" Width="63.199193405502214" Height="25.000000000000107" ZOrder="32915" FontSize="12" Valign="Middle" /> <Xref Database="Ensembl" ID="ENSG00000078674" /> </DataNode> <DataNode TextLabel="KIAA0753" GraphId="cb915" Type="GeneProduct"> <Comment>OFD1- And FOPNL-Interacting Protein</Comment> <Graphics CenterX="510.0039407200668" CenterY="781.9349872178319" Width="79.30737188054123" Height="22.15330912630374" ZOrder="32916" FontSize="12" Valign="Middle" /> <Xref Database="Ensembl" ID="ENSG00000198920" /> </DataNode> <DataNode TextLabel="PLK1" GraphId="bdbe7" Type="GeneProduct"> <Comment>Ppolo-like kinase 1 - ser/thr kinase</Comment> <Graphics CenterX="623.6400102691982" CenterY="781.9349872178318" Width="79.30737188054125" Height="22.153309126303796" 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