Copper levels can be evaluated to help diagnose several disease processes. These conditions may be monitored by looking at the total copper, the free serum copper, 24-hour urine copper, and liver biopsy copper concentrations. Serum ceruloplasmin is also a valuable test and can be used to determine the free serum copper.
Copper reference ranges are as follows:
Normal copper values mean that the individual has normal physiology, absorption, excretion, and dietary intake of copper.
Copper is found in many food sources such as seeds, organ meats, nuts, seafood, and liver.  Furthermore, copper is also found in the water supply. [3, 4] The average daily copper intake in 2001 was 1.54-1.70 mg/d in men and 1.13-1.18 mg/d in women.  With a wide variety of dietary sources, becoming copper deficient is difficult. 
However, copper deficiency may occur due to malabsorption, primarily in the duodenum, where most copper is absorbed. Other conditions that can cause a low copper level can be nephrotic syndrome and individuals with Menkes disease. Overcorrection of copper level in case of treatment for Wilson disease may also result in a copper deficiency. 
Conversely, a high value of total copper may indicate copper toxicity from ingesting too much copper, or, as is more common in infants, poor excretion secondary to underdeveloped biliary systems.  In the case of Wilson disease, liver biopsy shows high levels of copper and is considered the criterion standard for diagnosis. Additionally, elevated levels of urinary copper collected with the 24-hour urine study may also indicate a positive diagnosis of Wilson disease. Low levels of serum ceruloplasmin and serum copper are common findings in Wilson disease.
Low levels of serum copper and serum ceruloplasmin may also suggest Menkes disease. They may also indicate a dietary insufficiency; however, this is unlikely given the surplus of copper found in food and water. Low levels of copper seen on liver biopsy and 24-hour urine may also point a clinician to the diagnosis of Menkes disease or copper deficiency. 
Collection and Panels
Serum copper levels may be collected at any time during the day and should be drawn into a dark blue – topped tube. The dark blue – top tube has a sodium EDTA additive and is used for evaluating trace metals in the blood.
The ceruloplasmin may also be drawn at any time during the day and should be drawn in a red-topped tube. The serum is separated by centrifugation from the red blood cells and analyzed.
With regards to liver biopsy, the patient should not eat (NPO) after midnight the night prior to the procedure. Additionally, coagulation studies (PT/PTT/INR) should be drawn and evaluated prior to the procedure to evaluate the risk of bleeding. As with many procedures, the risk of bleeding, infection, and perforation of nearby organs exists.  The biopsy should be performed transcutaneously, and a core of tissue should be obtained and placed in a container that does not have any copper components.  The sample should be dried and frozen overnight for shipment to the lab.  The liver biopsy should be sent for a copper assay, which quantifies the amount of copper and is reported in either μmol/g of tissue or μg/g of tissue. [1, 9]
The 24-hour urine should be collected after the first urination upon waking, which is not voided into the collection device. Afterwards, the patient should be instructed to urinate entirely into the collection device provided. The following morning, the first urination attempt should be collected and is the last quantity collected for the study.  The collection device used is the same that is used for other 24-hour urine studies.