{"id":907,"date":"2025-04-08T16:13:39","date_gmt":"2025-04-08T21:13:39","guid":{"rendered":"https:\/\/wp.uthscsa.edu\/chromosome-18\/?page_id=907"},"modified":"2025-04-08T16:13:39","modified_gmt":"2025-04-08T21:13:39","slug":"clinical-dosage-map-legend-2","status":"publish","type":"page","link":"https:\/\/wp.uthscsa.edu\/chromosome-18\/clinical-dosage-map-legend-2\/","title":{"rendered":"Clinical Dosage Map Legend"},"content":{"rendered":"

[vc_row][vc_column width=”2\/3″][vc_column_text css=””]<\/p>\n

This map is best viewed on a screen larger than a mobile phone due to the amount of information presented.<\/em><\/strong><\/p>\n

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    1. Select either deletion or duplication.<\/li>\n
    2. Select the Genomic Build Version. This should be indicated on your genomics lab report next to the coordinates of the deletion or duplication.<\/li>\n
    3. Type in the coordinates of the deletion or duplication. The region you selected will be indicated by an orange bar to the left of chromosome picture. If you do not know the coordinates or the Genomic Build Version, you can find them on your microarray report from the clinical diagnostic lab. Instructions for interpreting that report are here: How to Read a Microarray Report<\/a><\/li>\n
    4. Select Genes or Phenotype Regions.<\/li>\n<\/ol>\n<\/li>\n<\/ol>\n

      If you selected Genes:<\/u><\/strong><\/p>\n

      The region you selected will be indicated by a green bar on the picture of the chromosome. The genes in the selected region which may have a clinical impact are shown in the window with 5 columns of information. The columns from left to right are:<\/p>\n

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